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. 2018 Jan 24;33(27):e75. doi: 10.3346/jkms.2018.33.e75

Table 1. Clinicopathological characteristics according to histologic subtypes of PTC.

Characteristics Classical (n = 1,374) Follicular variant (n = 22) Diffuse sclerosing variant (n = 10) Tall cell variant (n = 5)
Age, yr 50.0 ± 11.2 53.8 ± 9.6 43.7 ± 15.1a,b 53.0 ± 21.7c
Sex, female 1,234 (89.8) 16 (72.7) 7 (70.0)a 3 (60.0)a
Tumor size, cm 0.9 ± 0.6 1.4 ± 1.3a 2.1 ± 1.2a,b 2.0 ± 1.1a,b
ETE 520 (37.8) 7 (31.8) 8 (80.0)a,b 3 (60.0)a,b
LNM 518 (37.7) 4 (18.2)a 9 (90.0)a,b 3 (60.0)a,b
Advanced stage 393 (28.6) 9 (40.9) 9 (90.0)a,b 4 (80.0)a,b
BRAFV600E mutation 850 (61.9) 6 (27.3)a 2 (20.0)a 3 (60.0)b,c

Statistical significance was tested by the χ2 test. Data are expressed as mean ± standard deviation and frequency (%) for categorical variables.

PTC = papillary thyroid carcinoma, ETE = extrathyroidal extension, LNM = lymph node metastasis, Advanced stage = American Joint Committee on Cancer (AJCC) stage III + IV.

aP < 0.05 vs. conventional PTC; bP < 0.05 vs. follicular variant PTC; cP < 0.05 vs. diffuse sclerosing variant PTC.